Inducible CreER ^T2 mouse lines for characterization of retinal bipolar cell subtypes

Bipolar cells relay visual signals from photoreceptor cells to ganglion cells in the retina. Fifteen bipolar cell subtypes have been identified in the mouse retina. These subtypes are classified as ON and OFF bipolar cells based on their response to light stimulus or rod and cone bipolar cells based on their connection to photoreceptor cells. However, the unique structural and functional role of these subtypes in the processing of visual information is not fully known due to the inadequate tools and models available for their characterization. In this study, to trace the lineage and characterize <i>Vsx1</i>, <i>Lhx3</i>, and <i>Lhx4</i> - expressing bipolar cell subtypes in developing and adult mouse retina, we developed inducible Cre lines under the promoter of <i>Vsx1</i>, <i>Lhx3</i>, and <i>Lhx4</i> and crossed them with ChR2EYFP reporter mice. Lineages of cells expressing <i>Vsx1</i>, <i>Lhx3</i>, and <i>Lhx4</i> after Cre induction in the adult and postnatal mouse retina were then characterized. ChR2EYFP expression driven by <i>Vsx1</i>-CreER^T2 was detected in type 2, 6, and 7 bipolar cells, <i>Lhx3</i>-CreER^T2 in type 1b, 2, and 6 bipolar cells, and <i>Lhx4</i>-CreER^T2 in type 2, 3, 4, and 5 bipolar cells as well as cone photoreceptor cells in the adult mouse retina. These bipolar cell subtype-specific inducible Cre mouse lines serve as efficient tools for elucidation of the mechanisms that control bipolar cell subtype development and function in the retina.